Canonical Allele Identifier: CA569080360

Gene: FBXL4

Linked Data

• dbSNP Id: rs1562213163
• gnomAD v2: 6-99322328-G-GAAACAA
• gnomAD v4: 6-98874452-G-GAAACAA
• MyVariant Identifiers: chr6:g.99322337_99322343delinsACAAAACAAAACA (hg19) ; chr6:g.98874461_98874467delinsACAAAACAAAACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874455_98874460dup , CM000668.2:g.98874455_98874460dup	GRCh38
NC_000006.11:g.99322331_99322336dup , CM000668.1:g.99322331_99322336dup	GRCh37
NC_000006.10:g.99429052_99429057dup	NCBI36
NG_033903.1:g.78549_78554dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1703-17_1703-12dup MANE Select	ENSP00000358247.1:n.1703-17_1703-12dup
ENST00000229971.2:c.1703-17_1703-12dup	ENSP00000229971.1:n.1703-17_1703-12dup
ENST00000369244.6:c.1703-17_1703-12dup	ENSP00000358247.1:n.1703-17_1703-12dup
NM_001278716.1:c.1703-17_1703-12dup	NP_001265645.1:n.1703-17_1703-12dup
NM_012160.4:c.1703-17_1703-12dup	NP_036292.2:n.1703-17_1703-12dup
NR_103836.1:n.1748-17_1748-12dup
XM_005266930.1:c.1631-17_1631-12dup	XP_005266987.1:n.1631-17_1631-12dup
XM_005266930.3:c.1631-17_1631-12dup	XP_005266987.1:n.1631-17_1631-12dup
XM_017010726.1:c.1703-17_1703-12dup	XP_016866215.1:n.1703-17_1703-12dup
XM_017010727.2:c.1631-17_1631-12dup	XP_016866216.1:n.1631-17_1631-12dup
XM_017010728.1:c.977-17_977-12dup	XP_016866217.1:n.977-17_977-12dup
NM_001278716.2:c.1703-17_1703-12dup MANE Select	NP_001265645.1:n.1703-17_1703-12dup
NR_103836.2:n.1688-17_1688-12dup
NM_012160.5:c.1703-17_1703-12dup	NP_036292.2:n.1703-17_1703-12dup